Publications by authors named "David A Tregouet"

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Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays.
Maria Eugenia de la Morena-Barrio, Pierre Suchon, Eva Marie Jacobsen, Nina Iversen, Antonia Miñano

Blood· July 2022

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Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy.
Nadine Suffee, Thomas Moore-Morris, Bernd Jagla, Nathalie Mougenot, Gilles Dilanian, David A Tregouet

Circ Res· May 2020

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Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Rainer Malik, Ganesh Chauhan, Matthew Traylor, Muralidharan Sargurupremraj, Yukinori Okada

Nat Genet· July 2019

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A large-scale exome array analysis of venous thromboembolism.
Sara Lindström, Jennifer A Brody, Constance Turman, Marine Germain, Traci M Bartz

Genet Epidemiol· June 2019

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Common Risk Factors Add to Inherited Thrombophilia to Predict Venous Thromboembolism Risk in Families.
Pierre Suchon, Noemie Resseguier, Manal Ibrahim, Alexia Robin, Geoffroy Venton

TH Open· January 2019

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Rainer Malik, Ganesh Chauhan, Matthew Traylor, Muralidharan Sargurupremraj, Yukinori Okada

Nat Genet· April 2018

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Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension.
Marine Germain, Mélanie Eyries, David Montani, Odette Poirier, Barbara Girerd

Nat Genet· May 2013

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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
Eric Villard, Claire Perret, Françoise Gary, Carole Proust, Gilles Dilanian, David A Tregouet

Eur Heart J· May 2011

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Effect of cytochrome P450 2C19 genotype on voriconazole exposure in cystic fibrosis lung transplant patients.
Maud Berge, Romain Guillemain, David A Trégouet, Catherine Amrein, Veronique Boussaud

Eur J Clin Pharmacol· March 2011

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The factor XII -4C>T variant and risk of common thrombotic disorders: A HuGE review and meta-analysis of evidence from observational studies.
Candice Y Johnson, Ashleigh Tuite, Pierre E Morange, David A Tregouet, France Gagnon

Am J Epidemiol· January 2011

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Genetic variations at the endocannabinoid type 1 receptor gene (CNR1) are associated with obesity phenotypes in men.
Paola Russo, Pasquale Strazzullo, Francesco P Cappuccio, David A Tregouet, Fabio Lauria

J Clin Endocrinol Metab· June 2007

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Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations.
Samy Hadjadj, Lise Tarnow, Carol Forsblom, Gbenga Kazeem, Michel Marre, David A Tregouet

J Am Soc Nephrol· April 2007

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Associations of PPARGC1A haplotypes with plaque score but not with intima-media thickness of carotid arteries in middle-aged subjects.
Bernhard Iglseder, Hannes Oberkofler, Thomas K Felder, Kerstin Klein, Bernhard Paulweber, David A Tregouet

Stroke· September 2006

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Quantification of thrombin activatable fibrinolysis inhibitor (TAFI) gene polymorphism effects on plasma levels of TAFI measured with assays insensitive to isoform-dependent artefact.
Corinne Frère, Pierre Emmanuel Morange, Noémie Saut, David Alexandre Tregouet, Mariana Grosley

Thromb Haemost· August 2005

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Gender-specific association of a perilipin gene haplotype with obesity risk in a white population.
Lu Qi, Haiqing Shen, Ilona Larson, Ernst J Schaefer, Andrew S Greenberg, David A Tregouet

Obes Res· November 2004

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Combined effects of genetic and environmental factors on insulin resistance associated with reduced fetal growth.
Delphine Jaquet, David A Trégouët, Thierry Godefroy, Viviane Nicaud, Didi Chevenne

Diabetes· December 2002

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